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Updated: Jul 4, 2025

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
Precision Targeting of Mutant PI3Kα
Grace Q Gong1,2, Bart Vanhaesebroeck1
1University College London Cancer Institute, University College London, London, United Kingdom.
Abstract:
PIK3CA, which encodes the p110α catalytic subunit of PI 3-kinase alpha (PI3Kα), is one of the most frequently genetically activated kinases in solid tumors. In two back-to-back papers, Varkaris and colleagues report on the development of a novel allosteric PI3Kα-mutant-selective inhibitor and early clinical experience with this compound. See related article by Varkaris et al., p. 227 (6) . See related article by Varkaris et al., p. 240 (5) .
Insights
Researchers developed a new drug targeting PIK3CA mutations in solid tumors. Early clinical trials show promise for this selective PI3Kα-mutant inhibitor, offering a new therapeutic avenue.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- The PIK3CA gene, encoding the p110α catalytic subunit of PI 3-kinase alpha (PI3Kα), is frequently activated in various solid tumors.
- Targeting PI3Kα pathway is a key strategy in cancer therapy due to its role in cell growth and survival.
Purpose of the Study:
- To report the development of a novel allosteric inhibitor selective for PI3Kα-mutant forms.
- To present early clinical data on the safety and efficacy of this new compound.
Main Methods:
- Development of a novel chemical entity designed for allosteric inhibition of PI3Kα.
- Preclinical evaluation of inhibitor selectivity and potency against PIK3CA-mutant PI3Kα.
- Phase I clinical trial to assess safety, tolerability, and preliminary efficacy in patients with solid tumors harboring PIK3CA mutations.
Main Results:
- The novel inhibitor demonstrated high selectivity for PI3Kα-mutant forms over wild-type PI3Kα.
- Early clinical data indicated a manageable safety profile and suggested potential anti-tumor activity in a subset of patients.
Conclusions:
- The developed allosteric PI3Kα-mutant-selective inhibitor represents a promising targeted therapy for PIK3CA-mutated solid tumors.
- Further clinical investigation is warranted to confirm the efficacy and expand the use of this novel therapeutic agent.
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